Epothilones C, D, E, and F, Preparation and Compositions

ABSTRACT

The present invention relates to epothilones C, D, E, and F, their preparation and their use for the production of therapeutic compositions and compositions for plant protection.

This application is a continuation of U.S. application Ser. No. 09/313,524, filed May 17, 1999, which is a continuation of International Application No. PCT/EP97/06442, filed Nov. 18, 1997. The disclosure of each of the above applications is incorporated by reference in its entirety.

The present invention relates to epothilones C, D, E and F, their preparation and their use for the production of therapeutic compositions and compositions for plant protection.

Epothilones C and D

According to one embodiment, the invention relates to epothilones [C and D] which are obtainable in that

(a) Sorangium cellulosum DSM 6773 is cultured in a manner known per se in the presence of an adsorber resin, (b) the adsorber resin is removed from the culture and washed with a water/methanol mixture, (c) the washed adsorber resin is eluted with methanol and the eluate is concentrated to give a crude extract, (d) the concentrate obtained is extracted with ethyl acetate, the extract is concentrated and partitioned between methanol and hexane, (e) the methanolic phase is concentrated to give a raffinate and the concentrate is fractionated on a Sephadex column, (f) a fraction containing metabolic products of the microorganism employed is obtained, (g) the fraction obtained is chromatographed on a C 18 reverse phase to a methanol/water mixture and, sequentially

-   -   after a first fraction containing epothilone A and     -   a second fraction containing epothilone B     -   a third fraction containing a first further epothilone and     -   a fourth fraction containing a second further epothilone are         obtained and         (h1) the epothilone of the first further fraction and/or         (h2) the epothilone of the second further fraction are isolated.

The invention further relates to an epothilone [C] of the empirical formula C₂₆H₃₉NO₅S, characterized by the ¹H-and ¹³C-NMR spectrum as in Table 1.

The invention furthermore relates to epothilone C of the formula:

Epothilone C R═H.

The invention furthermore relates to epothilone [D] of the empirical formula C₂₇H₄₁NO₅S, characterized by the ¹H-and ¹³C-NMR spectrum as in Table 1.

The invention furthermore relates to epothilone D of the formula:

Epothilone D R═CH₃.

Epothilones C and D can be used for the preparation of the compounds of the following formula 1, where for their derivatization reference can be made to the derivatization methods described in WO-A-97/19 086.

In the above formula 1: R═H, C₁₋₄-alkyl; R¹, R², R³, R⁴, R⁵═H, C₁₋₆-alkyl,

-   -   C₁₋₆-acylbenzoyl,     -   C₁₋₄-trialkylsilyl,     -   benzyl,     -   phenyl,     -   C₁₋₆-alkoxy-,     -   C₆-alkyl-, hydroxy- and halogen-substituted benzyl or phenyl;         where two of the radicals R¹ to R⁵ can also combine to form the         group —(CH₂)_(n)— with n=1 to 6 and the alkyl or acyl groups         contained in the radicals are straight-chain or branched         radicals; Y and Z are either identical or different and are each         hydrogen, halogen, such as F, Cl, Br or I, pseudohalogen, such         as —NCO, —NCS or —N₃, OH, O—(C₁₋₆)-acyl, O—(C₁₋₆)-alkyl,         O-benzoyl. Y and Z can also be the O atom of an epoxide,         epothilone A and B not being claimed, or form one of the C—C         bonds of a C═C double bond.

Thus the 12, 13-double bond can be selectively

-   -   hydrogenated, for example catalytically or with diamine, a         compound of the formula 1 being obtained with Y=Z=H; or     -   epoxidized, for example with dimethyldioxirane or a peracid, a         compound of the formula 1 being obtained with Y and Z=—O—; or     -   converted into the dihalides, dipseudohalides or diazides, a         compound of the formula 1 being obtained with Y and Z=Hal,         pseudo-hal or N₃.

Epothilones E and F

According to a further embodiment the invention relates to a biotransformant of epothilone A, which is obtainable in that

(a) Sorangium cellulosum DSM 6773 is cultured in a manner known per se in the presence of an adsorber resin, removed from the adsorber resin and, if appropriate, the total amount or a part of the separated culture is treated with a methanolic solution of epothilone A,

(b) the culture treated with epothilone A is incubated and then treated with adsorber resin,

(c) the adsorber resin is separated from the culture, eluted with methanol and the eluate is concentrated to give a crude extract,

(d) the crude extract is partitioned between ethyl acetate and water, the ethyl acetate phase is separated off and concentrated to give an oil,

(e) the oil is chromatographed on a reverse phase under the following conditions:

column material: Nucleosil 100 C-18 7 μm column dimensions: 250 × 16 mm eluent: methanol/water = 60:40 flow rate: 10 ml/min and fractions having a content of biotransformant and which can be detected by UV extinction at 254 nm and have an R_(t) value of 20 min are separated off and the biotransformants are isolated.

The invention furthermore relates to a biotransformant of epothilone A of this type, which is obtainable in that in stage (a) a culture is separated off which is three or four or more days old.

The invention furthermore relates to a biotransformant of epothilone A of this type, which is obtainable in that in stage (b) incubation is carried out for one or two or more days.

The invention furthermore relates to a compound of the empirical formula C₂₆H₃₉NO₇S, characterized by the following ¹H-NMR spectrum (300 MHz, CDCl₃): delta=2.38 (2-H_(a)), 2.51 (2-H_(b)), 4.17 (3-H), 3.19 (6-H), 3.74 (7-H), 1.30-1.70 (8-H, 9-H₂, 10-H₂, 11-H₂), 2.89 (12-H), 3.00 (13-H), 1.88 (14-H_(a)), 2.07 (14-H_(b)), 5.40 (15-H), 6.57 (17-H), 7.08 (19-H), 4.85 (21-H₂), 1.05 (22-H₃), 1.32 (23-H₃), 1.17 (24-H₃), 0.97 (25-H₃), 2.04 (27-H₃).

The invention furthermore relates to a compound (epothilone E) of the formula:

Epothilone E R═H

According to a further embodiment, the invention relates to a biotransformant of epothilone B, which is obtainable in that

-   -   (a) Sorangium cellulosum DSM 6773 is cultured in a manner known         per se in the presence of an adsorber resin, separated from the         adsorber resin and, if appropriate, the total amount or a part         of the separated culture is treated with a methanolic solution         of epothilone B,     -   (b) the culture treated with epothilone B is incubated and then         treated with adsorber resin,     -   (c) the adsorber resin is separated from the culture, eluted         with methanol and the eluate is concentrated to give a crude         extract,     -   (d) the crude extract is partitioned between ethyl acetate and         water, the ethyl acetate phase is separated off and concentrated         to give an oil,     -   (e) the oil is chromatographed on a reverse phase under the         following conditions:

column material: Nucleosil 100 C-18 7 μm column dimensions: 250 × 16 mm eluent: methanol/water = 60:40 flow rate: 10 ml/min and fractions having a content of biotransformant and which can be detected by UV extinction at 254 nm and have an R_(t) value of 24.5 min are separated off and the biotransformants are isolated.

The invention furthermore relates to a biotransformant of epothilone B of this type, which is obtainable in that in stage (a) a culture is separated off which is three or four or more days old.

The invention furthermore relates to a biotransformant of epothilone B of this type, which is obtainable in that in stage (b) incubation is carried out for one or two or more days.

The invention furthermore relates to a compound of the empirical formula C₂₇H₄₁NO₇S, characterized by the following ¹H-NMR spectrum (300 MHz, CDCl₃): delta=2.37 (2-H_(a)), 2.52 (2-H_(b)), 4.20 (3-H), 3.27 (6-H), 3.74 (7-H), 1.30-1.70 (8-H, 9-H₂, 10-H₂, 11-H₂), 2.78 (13-H), 1.91 (14-H), 2.06 (14-H_(b)), 5.42 (15-H), 6.58 (17-H), 7.10 (19-H), 4.89 (21-H₂), 1.05 (22-H₃), 1.26 (23-H₃), 1.14 (24-H₃), 0.98 (25-H₃), 1.35 (26-H₃), 2.06 (27-H₃).

The invention furthermore relates to a compound (epothilone F) of the formula:

Epothilone F R═CH₃

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows a HPLC analysis of an XAD eluate at the end of a fermentation.

FIG. 2 shows an enrichment of epothilone E and F in a fermentation broth after feeding of a mixture of epothilone A and B, analysed after incubation for 48 hours.

FIG. 3 shows kinetics of the biotransformation of epothilone A to epothilone E by Sorangium cellulosum So ce90.

FIG. 4 shows biotransformation of epothilone A to epothilone E.

FIG. 5 shows biotransformation of epothilone B to epothilone F.

PREPARATION AND COMPOSITIONS

The compounds or epothilones according to the invention are obtainable by the abovementioned measures.

The invention furthermore relates to compositions for plant protection in agriculture, forestry and/or horticulture, consisting of one or more of the abovementioned epothilones C, D, E and F or consisting of one or more of the abovementioned epothilones in addition to one or more customary carrier(s) and/or diluent(s).

The invention finally relates to therapeutic compositions, consisting of one or more of the abovementioned compounds or one or more of the above-mentioned compounds in addition to one or more customary carrier(s) and/or diluent(s). In particular, these compositions can show cytotoxic activities and/or bring about immunosuppression and/or be employed for the control of malignant tumours, it being particularly preferably possible for them to be used as cytostatics.

In the following, the invention is illustrated and described in greater detail by the description of some selected working examples.

EXAMPLES Example 1 Epothilones C and D A. Production Strain and Culture Conditions According to the Epothilone Basic Patent DE-B-41 38 042.

B. Production with DSM 6773

75 l of culture are grown as described in the basic patent and used for the inoculation of a production fermenter with 700 l of production medium consisting of 0.8% starch, 0.2% glucose, 0.2% soya flour, 0.2% yeast extract, 0.1% CaCl₂×2H₂O, 0.1% MgSO₄×7H₂O, 8 mg/l of Fe-EDTA, pH=7.4 and optionally 15 l of Amberlite XAD-16 adsorber resin. The fermentation lasts 7-10 days at 30 C, aeration with 2 m³/hr. By controlling the speed of rotation, the pO₂ is kept at 30%.

C. Isolation

The adsorber resin is separated from the culture using a 0.7 m², 100 mesh process filter and freed from polar concomitants by washing with 3 bed volumes of water/methanol 2:1. By elution with 4 bed volumes of methanol, a crude extract is obtained which is evaporated in vacuo until the water phase appears. This is extracted three times with the same volume of ethyl acetate. Evaporation of the organic phase affords 240 g of crude extract, which is partitioned between methanol and heptane in order to separate off lipophilic concomitants. By evaporation in vacuo, 180 g of raffinate are obtained from the methanol phase and are fractionated into three portions on Sephadex LH-20 (column 20×100 cm, 20 ml/min of methanol). The epothilones are contained in the fraction of a total of 72 g eluted with a 240-300 min retention time. To separate the epothilones, the fraction is chromatographed in three portions on Lichrosorb RP-18 (15 μm, column 10×40 cm, eluent 180 ml/min methanol/water 65:35). After epothilone A and B, epothilone C, with R_(t)=90-95 min, and epothilone D, 100-110 min, are eluted and after evaporation in vacuo obtained in a yield of 0.3 g each as colourless oils.

D. Physical Properties

Epothilone C R═H

Epothilone D R═CH₃

Epothilone C

C₂₆H₃₉NO₅S [477]

ESI-MS: (positive ions): 478.5 for [M+H]⁺

1H and 13C see NMR table

TLC: R_(f)=0.82

TLC aluminum foil 60 F 254 Merck, eluent: dichloromethane/methanol=9:1

Detection: UV extinction at 254 nm. Spraying with vanillin-sulphuric acid reagent, blue-grey coloration on heating to 120° C.

HPLC: R_(t)=11.5 min

Column: Nucleosil 100 C-18 7 μm, 125×4 mm

Eluent: methanol/water=65:35

Flow rate: 1 ml/min

Detection: diode array

Epothilone D

C₂₇H₄₁NO₅S [491]

ESI-MS: (positive ions): 492.5 for [M+H]⁺

1H and 13C see NMR table

TLC: R_(f)=0.82

TLC aluminum foil 60 F 254 Merck, eluent: dichloromethane/methanol=9:1

Detection: UV extinction at 254 nm. Spraying with vanillin-sulphuric acid reagent, blue-grey coloration on heating to 120° C.

HPLC: R_(t)=15.3 min

Column: Nucleosil 100 C-18 7 μm, 125×4 mm

Eluent: methanol/water=65:35

Flow rate: 1 ml/min

Detection: diode array

TABLE 1 ¹H- and ¹³C-NMR data of epothilone C and epothilone D in [D₆] DMSO at 300 MHz Epothilone C Epothilone D δ δ δ δ H atom (ppm) C atom (ppm) (ppm) C atom (ppm) 1 170.3 1 170.1  2-Ha 2.38 2 38.4 2.35 2 39.0  2-Hb 2.50 3 71.2 2.38 3 70.8  3-H 3.97 4 53.1 4.10 4 53.2  3-OH 5.12 5 217.1 5.08 5 217.4  6-H 3.07 6 45.4 3.11 6 44.4  7-H 3.49 7 75.9 3.48 7 75.5  7-OH 4.46 8 35.4 4.46 8 36.3  8-H 1.34 9 27.6 1.29 9 29.9  9-Ha 1.15 10 30.0 1.14 10 25.9  9-Hb 1.40 11 27.6 1.38 11 31.8* 10-Ha 1.15* 12 124.6 1.14* 12 138.3 10-Hb 1.35* 13 133.1 1.35* 13 120.3 11-Ha 1.90 14 31.1 1.75 14 31.6* 11-Hb 2.18 15 76.3 2.10 15 76.6 12-H 5.38** 16 137.3 16 137.2 13-H 5.44** 17 119.1 5.08 17 119.2 14-Ha 2.35 18 152.1 2.30 18 152.1 14-Hb 2.70 19 117.7 2.65 19 117.7 15-H 5.27 20 164.2 5.29 20 164.3 17-H 6.50 21 18.8 6.51 21 18.9 19-H 7.35 22 20.8 7.35 22 19.7 21-H₃ 2.65 23 22.6 2.65 23 22.5 22-H₃ 0.94 24 16.7 0.90 24 16.4 23-H₃ 1.21 25 18.4 1.19 25 18.4 24-H₃ 1.06 27 14.2 1.07 26 22.9 25-H₃ 0.90 0.91 27 14.1 26-H₃ 1.63 27-H₃ 2.10 2.11 *, **assignment interchangeable

Example 2 Epothilone A and 12,13-bisepi-epothilone A from Epothilone C

50 mg of epothilone A are dissolved in 1.5 ml of acetone and treated with 1.5 ml of a 0.07 molar solution of dimethyldioxirane in acetone. After standing at room temperature for 6 hours, the mixture is evaporated in vacuo and the residue is separated by preparative HPLC on silica gel (eluent: methyl tert-butyl ether/petroleum ether/methanol 33:66:1).

Yield:

25 mg of epothilone A, R_(t)=3.5 min (analyt. HPLC, 7 μm, column 4×250 mm, eluent see above, flow rate 1.5 ml/min) and

20 mg of 12,13-bisepi-epothilone A, R_(t)=3.7 min, ESI-MS (pos. ions) m/e=494 [M+H]⁺

¹H-NMR in [D₄] methanol, selected signals: delta=4.32 (3-H), 3.79 (7-H), 3.06 (12-H), 3.16 (13-H), 5.54 (15-H), 6.69 (17-H), 1.20 (22-H), 1.45 (23-H).

12,13-bisepi-epothilone A R═H

Example 3 Epothilone E and F, Novel Biotransformation Products of Epothilones A and B Production Strain

The production strain Sorangium cellulosum So ce90 was isolated in July 1985 in GBF from a soil sample from the banks of the Zambesi and deposited on Oct. 28, 1991 in the German Collection for Microorganisms under No. DSM 6773.

The characterization of the producer and the culture conditions are described in: Höfle, G.; N. Bedorf, K. Gerth & H. Reichenbach: Epothilones, processes for their preparation and compositions containing them. DE 41 38 042 A1, laid open on 27 May 1993.

Formation of Epothilones E and F During Fermentation:

A typical fermentation proceeds in the following manner: A 100 l bioreactor is filled with 60 l of medium (0.8% starch; 0.2% glucose; 0.2% soya flour; 0.2% yeast extract; 0.1% CaCl₂×2H₂O; 0.1% MgSO₄×7H₂O; 8 mg/l of Fe-EDTA; pH 7.4). 2% of adsorber resin (XAD-16, Rohm & Haas) are additionally added. The medium is sterilized by autoclaving (2 hours, 120° C.). Inoculation is carried out with 10 l of a preculture grown in the same medium (additionally 50 mM HEPES buffer pH 7.4) in a shaker flask (160 rpm, 30° C.). Fermentation is carried out at 32° C. with a stirrer speed of 500 rpm and an introduction of 0.2 N1 per m³ per hour of air, the pH is kept at 7.4 by addition of KOH. The fermentation lasts 7 to 10 days. The epothilones formed are continuously bound to the adsorber resin during the fermentation. After separating off the culture broth (e.g. by screening in a process filter), the resin is washed with 3 bed volumes of water and eluted with 4 bed volumes of methanol. The eluate is concentrated to dryness and taken up in 700 ml of methanol.

HPLC Analysis of the XAD Eluate:

In relation to the starting volume of the reactor (70 l), the eluate is concentrated 100:1. The analysis is carried out using a 1090 HPLC unit from Hewlett Packard. To separate the constituents, a microbore column (125/2 Nucleosil 120-5 C₁₈) from Machery-Nagel (Düren) is used. Elution is carried out using a gradient of water/acetonitrile from initially 75:25 up to 50:50 after 5.5 minutes. This ratio is maintained up to the 7th minute, in order to then increase it up to the 10th minute to 100% acetonitrile.

Measurement is carried out at a wavelength of 250 nm and a bandwidth of 4 nm. The diode array spectra are measured in the wavelength range from 200 to 400 nm. In the XAD eluate, two novel substances with R_(t) 5.29 and R_(t) 5.91 stand out, whose adsorption spectra are identical with those of epothilones A and B (FIG. 1; E corresponds to A, F corresponds to B). These substances are only formed in traces under the given fermentation conditions.

Biotransformation of Epothilone A and B to Epothilone E and F:

A 500 ml culture of So ce90, 4 days old and maintained with adsorber resin, is used for the specific biotransformation. 250 ml of this are transferred to a sterile 1 l Erlenmeyer flask leaving behind the XAD. A methanolic solution of a mixture of a total of 36 mg of epothilone A+14 mg of B is then added and the flask is incubated on a shaking rack for two days at 30° C. and 200 rpm. The formation of the epothilones E and F is analysed directly from 10 μl of the centrifuged culture supernatant (FIG. 2). The conversion takes place only in the presence of the cells and is dependent on the cell densities employed and the time. Kinetics of the conversion are shown for epothilone A in FIG. 3.

Isolation of Epothilone E and F

To isolate epothilone E and F, three shaker flask batches from the biotransformation (see above) are combined and shaken with 20 ml of XAD-16 for 1 h. The XAD is obtained by screening and eluted with 200 ml of methanol. The eluate is evaporated in vacuo to give 1.7 g of crude extract. This is partitioned between 30 ml of ethyl acetate and 100 ml of water. On evaporation in vacuo, 330 mg of an oily residue are obtained from the ethyl acetate phase, which are chromatographed in five runs on a 250×20 mm RP-18 column (eluent: methanol/water 58:42, detection 254 nm).

Yield: epothilone E 50 mg F 10 mg

Biological Action of Epothilone E:

In cell cultures, the concentration was determined which reduces the growth by 50% (IC₅₀) and compared with the values for epothilone A.

IC50 (ng/ml) Cell line Epothilone E Epothilone A HeLa.KB-3.1 (human) 5 1 Mouse fibroblasts, L929 20 4

Epothilone E

C₂₆H₃₉HO₇S [509]

ESI-MS: (positive ions): 510.3 for [M+H]⁺

TLC: R_(f)=0.58

TLC aluminum foil 60 F 254 Merck, eluent: dichloromethane/methanol=9:1

Detection: UV extinction at 254 nm. Spraying with vanillin-sulphuric acid reagent, blue-grey colouration on heating to 120° C.

HPLC: R_(t)=5.0 min

Column: Nucleosil 100 C-18 7 μm, 250×4 mm

Eluent: methanol/water=60:40

Flow rate: 1.2 ml/min

Detection: diode array

¹H-NMR (300 MHz, CDCl₃): delta=2.38 (2-H_(a)), 2.51 (2-H_(b)), 4.17 (3-H), 3.19 (6-H), 3.74 (7-H), 1.30-1.70 (8-H, 9-H₂, 10-H₂, 11-H₂), 2.89 (12-H), 3.00 (13-H), 1.88 (14-H_(a)), 2.07 (14-H_(b)), 5.40 (15-H), 6.57 (17-H), 7.08 (19-H), 4.85 (21-H₂), 1.05 (22-H₃), 1.32 (23-H₃), 1.17 (24-H₃), 0.97 (25-H₃), 2.04 (27-H₃)

Epothilone F

C₂₇H_(X)41NO₇S [523]

ESI-MS: (positive ions): 524.5 for [M+H]⁺

TLC: R_(f)=0.58

TLC aluminum foil 60 F 254 Merck, eluent: dichloromethane/methanol=9:1

Detection: UV extinction at 254 nm. Spraying with vanillin-sulphuric acid reagent, blue-grey colouration on heating to 120° C.

HPLC: R_(t)=5.4 min

Column: Nucleosil 100 C-18 7 μm, 250×4 mm

Eluent: methanol/water=60:40

Flow rate: 1.2 m/min

Detection: diode array

¹H-NMR (300 MHz, CDCl₃): delta=2.37 (2-H_(a)), 2.52 (2-H_(b)), 4.20 (3-H), 3.27 (6-H), 3.74 (7-H), 1.30-1.70 (8-H, 9-H₂, 10-H₂, 11-H₂), 2.78 (13-H), 1.91 (14-H), 2.06 (14-H_(b)), 5.42 (15-H), 6.58 (17-H), 7.10 (19-H), 4.89 (21-H₂), 1.05 (22-H₃), 1.26 (23-H₃), 1.14 (24-H₃), 0.98 (25-H₃), 1.35 (26-H₃), 2.06 (27-H₃).

Example 4 Preparation of Epothilone E and F by Biotransformation with Sorangium cellulosum So ce90 1) Carrying out the Biotransformation:

For the biotransformation, a culture of Sorangium cellulosum So ce90 is used which has been shaken for four days in the presence of 2% XAD 16 adsorber resin (Rohm and Haas, Frankfurt/M.) at 30° C. and 160 rpm. The culture medium has the following composition in g/litre of distilled water: potato starch (Maizena), 8; glucose (Maizena), 8; defatted soya flour, 2; yeast extract (Marcor), 2; ethylenediaminetetraacetic acid, iron(III) sodium salt, 0.008; MgSO₄×7H₂O, 1; CaCl₂×2H₂O, 1; HEPES 11.5. The pH is adjusted to 7.4 before autoclaving with KOH. The XAD is separated from the culture by sieving through a stainless steel sieve (200 μm mesh width). The bacteria are sedimented by centrifugation for 10 min at 10,000 rpm and the pellet is resuspended in ⅕ of the culture supernatant. Epothilone A or epothilone B in methanolic solution is then added to the concentrated bacterial suspension in a concentration of 0.5 g/litre. The culture is cultured further as described above. To analyse the biotransformation, a 1 ml sample is taken at the desired times, 0.1 ml of XAD is added and the sample is shaken at 30° C. for 30 min. The XAD is eluted with methanol. The eluate is concentrated to dryness and taken up again in 0.2 ml of methanol. This sample is analysed by means of HPLC.

FIG. 4) Kinetics of the biotransformation of epothilone A to epothilone E

FIG. 5) Kinetics of the biotransformation of epothilone B to epothilone F.

2) Preparation of Epothilone E by Biotransformation of 1 g of Epothilone A.

The strain Sorangium cellulosum So ce90 is grown for four days in 8.5 l of the above medium (but without XAD addition) in a 10 litre bioreactor at 30° C., a speed of rotation of 150 rpm and an introduction of 11/min of air.

The culture is then concentrated to 3 l by crossflow filtration. For this purpose, 0.6 m² of a membrane having a pore size of 0.3 μm are used.

The concentrated culture is transferred to a 4 litre bioreactor and a methanolic solution of 1 g of epothilone A in 10 ml of methanol is added. The culture is then cultured further for a period of time of 21.5 h. The temperature is 32° C., the stirrer speed is 455 rpm and the introduction of air takes place at 6 μl/min. At the time of harvesting, 100 ml of XAD is added and the mixture is incubated further for 1 h. The XAD is separated from the cells by screening and exhaustively eluted with methanol. The concentrated eluate is analysed by means of HPLC.

Balancing of the Biotransformation:

Epothilone A employed: 1000 mg=100% Epothilone A recovered after 21.5 h: 53.7 mg=5.4% Epothilone E formed after 21.5 h: 661.4 mg=66.1% Epothilone A completely decomposed:=28.5%

Experiment 5

The epothilones according to the invention were tested with cell cultures (Table 2) and for promotion of polymerization (Table 3).

TABLE 2 Epothilone tests with cell cultures Epothilone A B C D E F 493 507 477 491 509 523 IC-50 [ng/ml] Mouse fibroblasts L 929 4 1 100 20 20 1.5 human tumor cell lines: HL-60 (leukaemia) 0.2 0.2 10 3 1 0.3 K-562 (leukaemia) 0.3 0.3 20 10 2 0.5 U-937 (lymphoma) 0.2 0.2 10 3 1 0.2 KB-3.1 (carcinoma of the 1 0.6 20 12 5 0.5 cervix) KB-V1 (carcinoma of the 0.3 0.3 15 3 5 0.6 cervix multires A-498 (carcinoma of the — 1.5 150 20 20 3 kidney) A-549 (carcinoma of the lung) 0.7 0.1 30 10 3 0.1

TABLE 3 Polymerization test with epothilones Parameter: Time up to the half-maximal polymerization of the control Agent Agent Measurement: w x y z [s] [%] Control 200 170 180 210 190 100 Epothilone A 95 60 70 70 74 39 Epothilone B 23 25 30 26 14 Epothilone C 125 76 95 80 94 49 Epothilone D 125 73 120 106 56 Epothilone E 80 60 50 45 59 31 Epothilone F 80 40 30 50 50 26 Standard Test with 0.9 mg of Tubulin/ml and 1 μM Sample Concentration

The polymerization test is an in vitro test using purified tubulin from pigs' brain. Evaluation is carried out photometrically. Polymerization-promoting substances such as the epothilones reduce the time up to which half-maximal polymerization has taken place, i.e. the shorter the time, the more active the compound. w, x, y and z are four independent experiments, the relative activity is expressed in the last column in % of the control; again the lowest values indicate the best activity. The ranking list corresponds reasonably accurately to that found in cell cultures. 

1. A compound having the formula

said compound having a state of purity such as to be substantially free of other major metabolic products produced by Sorangium cellulosum.
 2. A compound having the formula

said compound having a state of purity such as to be substantially free of other major metabolic products produced by Sorangium cellulosum.
 3. A composition for plant protection in agriculture, forestry or horticulture comprising a compound according to claim 1 in combination with at least one agriculturally, forestrally or horticulturally acceptable carrier or diluent.
 4. A composition for plant protection in agriculture, forestry or horticulture comprising a compound according to claim 2 in combination with at least one agriculturally, forestrally or horticulturally acceptable carrier or diluent.
 5. A therapeutic composition comprising a compound according to claim 1 in combination with a pharmaceutically acceptable carrier or diluent.
 6. A therapeutic composition comprising a compound according to claim 2 in combination with a pharmaceutically acceptable carrier or diluent. 